IP Library Granted Patent US 7,741,300
Granted Patent B2
US 7,741,300 · App. 11/320,019 · Granted Jun 22, 2010

Methods of using nucleic acid vector-lipid complexes

Assignee: National Jewish Medical and Research Center
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,741,300
App. No.
11/320,019
Granted
Jun 22, 2010
Kind
B2
Abstract

This invention relates to a vaccine and a method for immune activation which is effective for eliciting both a systemic, non-antigen specific immune response and a strong antigen-specific immune response in a mammal. The method is particularly effective for protecting a mammal from a disease including cancer, a disease associated with allergic inflammation, an infectious disease, or a condition associated with a deleterious activity of a self-antigen. Also disclosed are therapeutic compositions useful in such a method.

Claims (11)

1. A method for eliciting a systemic, non-antigen-specific immune response in a mammal, comprising administering to said mammal an amount of a composition effective to elicit said immune response, wherein said composition comprises:

a. a cationic liposome delivery vehicle; and

b. an isolated nucleic acid molecule comprising an isolated bacterially-derived nucleic acid vector without a gene insert or a fragment thereof.

2. The method of claim 1 , wherein said liposome delivery vehicle comprises lipids selected from the group consisting of multilamellar vesicle lipids and extruded lipids.

3. The method of claim 1 , wherein said liposome delivery vehicle comprises multilamellar vesicle lipids.

4. The method of claim 1 , wherein said liposome delivery vehicle comprises pairs of lipids selected from the group consisting of DOTMA and cholesterol; DOTAP and cholesterol; DOTIM and cholesterol, and DDAB and cholesterol.

5. The method of claim 1 , wherein said liposome delivery vehicle comprises DOTAP and cholesterol.

6. The method of claim 1 , wherein said composition further comprises a pharmaceutically acceptable excipient.

7. The method of claim 6 , wherein said excipient comprises a non-ionic diluent.

8. The method of claim 7 , wherein said excipient is 5 percent dextrose in water.

9. The method of claim 1 , wherein said composition has a nucleic acid to lipid ratio of from about 1:1 to about 1:64.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Oct 6, 2015
From: TRIPLEPOINT CAPITAL LLC
To: JUVARIS BIOTHERAPEUTICS, INC.
Reel/Frame 036739/0195 →
SECURITY AGREEMENT Recorded Oct 4, 2011
From: JUVARIS BIOTHERAPEUTICS, INC.
To: TRIPLEPOINT CAPITAL LLC
Reel/Frame 027015/0765 →
Continuity (3)
Continuation 1001259700 · Nov 30, 2001
Continuation In Part 0910475900 · Jun 25, 1998
Related Publication 20060223769A1 · Oct 5, 2006